Prospective Patient Reported Outcomes (PRO) Registry in Patients With Advanced Renal Cell Carcinoma
PROKidney
Open-labeled, Multicenter, Non-interventional, Prospective PRO Registry for Patients With First Line Treatment for Advanced RCC Using a Tablet-technology Based Digital Device
1 other identifier
observational
98
1 country
1
Brief Summary
Evaluation of patient reported outcomes ( PRO) regarding typical ailments in the REAL LIFE Renal Cell Carcinoma population
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Aug 2015
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 19, 2015
CompletedFirst Submitted
Initial submission to the registry
August 26, 2015
CompletedFirst Posted
Study publicly available on registry
September 2, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 19, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
February 19, 2021
CompletedMarch 25, 2021
March 1, 2021
5.5 years
August 26, 2015
March 24, 2021
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Primary Outcome Measure (Patient Reported Outcomes (PRO) regarding typical ailments in the real Life RCC population)
Patient Reported Outcomes (PRO) regarding typical ailments in the real Life RCC population
24 months
Secondary Outcomes (1)
Secondary Outcome Measures (Patient Reported Outcomes (PRO) regarding the impact of treatment on daily life)
24 months
Eligibility Criteria
Patient with advanced (inoperable or metastatic) renal cell cancer at the start of the first line antitumoral therapy
You may qualify if:
- Histologically confirmed renal cell carcinoma
- Start of the first line systemic treatment
- Ability to read and understand German
- Written informed consent
You may not qualify if:
- None
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- iOMEDICO AGlead
Study Sites (1)
Multiple sites all over Germany
Multiple Locations, Germany
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Tilman Kirste, MD
medical practise for oncology
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 26, 2015
First Posted
September 2, 2015
Study Start
August 19, 2015
Primary Completion
February 19, 2021
Study Completion
February 19, 2021
Last Updated
March 25, 2021
Record last verified: 2021-03
Data Sharing
- IPD Sharing
- Will not share